PT719772E - Derivado de imidazolidinona opticamente activo e processo. - Google Patents

Derivado de imidazolidinona opticamente activo e processo. Download PDF

Info

Publication number: PT719772E
Authority: PT; Portugal
Prior art keywords: carbon atoms; groups; imidazolidinone; general formula; addition salts
Prior art date: 1993-09-17

Application number

PT94926387T

Other languages

English (en)

Portuguese (pt)

Inventor

Yasuo Takano

Kei Okazaki

Takashi Hirayama

Tsuyoshi Anraku

Original Assignee

Kyorin Seiyaku Kk

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1993-09-17

Filing date

1994-09-12

Publication date

2000-11-30

1994-09-12 Application filed by Kyorin Seiyaku Kk filed Critical Kyorin Seiyaku Kk

2000-11-30 Publication of PT719772E publication Critical patent/PT719772E/pt

Links

238000000034 method Methods 0.000 title abstract description 22
230000008569 process Effects 0.000 title abstract description 7
YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 title description 2
-1 nitro, amino Chemical group 0.000 claims abstract description 25
125000000217 alkyl group Chemical group 0.000 claims abstract description 13
150000003839 salts Chemical class 0.000 claims abstract description 13
150000008624 imidazolidinones Chemical class 0.000 claims abstract description 10
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 5
229910052736 halogen Inorganic materials 0.000 claims abstract description 3
150000002367 halogens Chemical class 0.000 claims abstract description 3
125000003545 alkoxy group Chemical group 0.000 claims abstract 7
125000004414 alkyl thio group Chemical group 0.000 claims abstract 3
125000004093 cyano group Chemical group *C#N 0.000 claims abstract 3
150000001875 compounds Chemical class 0.000 claims description 85
239000002253 acid Substances 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 17
125000003277 amino group Chemical group 0.000 claims description 13
125000005843 halogen group Chemical group 0.000 claims description 12
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 1
229940005524 anti-dementia drug Drugs 0.000 claims 1
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239000001257 hydrogen Substances 0.000 abstract description 4
150000002431 hydrogen Chemical class 0.000 abstract description 2
UQOFGTXDASPNLL-XHNCKOQMSA-N Muscarine Chemical compound C[C@@H]1O[C@H](C[N+](C)(C)C)C[C@H]1O UQOFGTXDASPNLL-XHNCKOQMSA-N 0.000 abstract 1
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239000002904 solvent Substances 0.000 description 52
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RMHMFHUVIITRHF-UHFFFAOYSA-N pirenzepine Chemical compound C1CN(C)CCN1CC(=O)N1C2=NC=CC=C2NC(=O)C2=CC=CC=C21 RMHMFHUVIITRHF-UHFFFAOYSA-N 0.000 description 11
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238000009835 boiling Methods 0.000 description 7
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VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
230000027455 binding Effects 0.000 description 6
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238000004821 distillation Methods 0.000 description 6
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150000004820 halides Chemical class 0.000 description 6
238000011084 recovery Methods 0.000 description 6
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
GVOCQRKNTWKJNU-CYBMUJFWSA-N 1-(4-fluorophenyl)-3-[(3r)-piperidin-3-yl]imidazolidin-2-one Chemical compound C1=CC(F)=CC=C1N1C(=O)N([C@H]2CNCCC2)CC1 GVOCQRKNTWKJNU-CYBMUJFWSA-N 0.000 description 5
230000006949 cholinergic function Effects 0.000 description 5
UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 5
125000006239 protecting group Chemical group 0.000 description 5
229940126585 therapeutic drug Drugs 0.000 description 5
HARWNWOLWMTQCC-GFCCVEGCSA-N (3r)-1-benzylpiperidin-3-amine Chemical compound C1[C@H](N)CCCN1CC1=CC=CC=C1 HARWNWOLWMTQCC-GFCCVEGCSA-N 0.000 description 4
238000005160 1H NMR spectroscopy Methods 0.000 description 4
FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 4
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 4
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241000699670 Mus sp. Species 0.000 description 4
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150000008065 acid anhydrides Chemical class 0.000 description 4
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229910000085 borane Inorganic materials 0.000 description 4
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QGRKPMMKWHYHSB-UHFFFAOYSA-N 1-(3-benzylpiperidin-1-yl)-3-(4-fluorophenyl)imidazolidin-2-one Chemical compound C1=CC(F)=CC=C1N1C(=O)N(N2CC(CC=3C=CC=CC=3)CCC2)CC1 QGRKPMMKWHYHSB-UHFFFAOYSA-N 0.000 description 2
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KVPWIJXNIOUOSG-GOSISDBHSA-N 1-[(3r)-3-benzylpiperidin-1-yl]-3-(4-chlorophenyl)imidazolidin-2-one Chemical compound C1=CC(Cl)=CC=C1N1C(=O)N(N2C[C@@H](CC=3C=CC=CC=3)CCC2)CC1 KVPWIJXNIOUOSG-GOSISDBHSA-N 0.000 description 1
QGRKPMMKWHYHSB-GOSISDBHSA-N 1-[(3r)-3-benzylpiperidin-1-yl]-3-(4-fluorophenyl)imidazolidin-2-one Chemical compound C1=CC(F)=CC=C1N1C(=O)N(N2C[C@@H](CC=3C=CC=CC=3)CCC2)CC1 QGRKPMMKWHYHSB-GOSISDBHSA-N 0.000 description 1
QGRKPMMKWHYHSB-SFHVURJKSA-N 1-[(3s)-3-benzylpiperidin-1-yl]-3-(4-fluorophenyl)imidazolidin-2-one Chemical compound C1=CC(F)=CC=C1N1C(=O)N(N2C[C@H](CC=3C=CC=CC=3)CCC2)CC1 QGRKPMMKWHYHSB-SFHVURJKSA-N 0.000 description 1
VZNCSZQPNIEEMN-UHFFFAOYSA-N 1-fluoro-2-isocyanatobenzene Chemical compound FC1=CC=CC=C1N=C=O VZNCSZQPNIEEMN-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
KMGUEILFFWDGFV-UHFFFAOYSA-N 2-benzoyl-2-benzoyloxy-3-hydroxybutanedioic acid Chemical compound C=1C=CC=CC=1C(=O)C(C(C(O)=O)O)(C(O)=O)OC(=O)C1=CC=CC=C1 KMGUEILFFWDGFV-UHFFFAOYSA-N 0.000 description 1
JJKWHOSQTYYFAE-UHFFFAOYSA-N 2-methoxyacetyl chloride Chemical compound COCC(Cl)=O JJKWHOSQTYYFAE-UHFFFAOYSA-N 0.000 description 1
229940100578 Acetylcholinesterase inhibitor Drugs 0.000 description 1
206010002091 Anaesthesia Diseases 0.000 description 1
206010003062 Apraxia Diseases 0.000 description 1
229930003347 Atropine Natural products 0.000 description 1
101100220553 Caenorhabditis elegans chd-3 gene Proteins 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
238000007167 Hofmann rearrangement reaction Methods 0.000 description 1
RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
208000020358 Learning disease Diseases 0.000 description 1
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
102000007205 Muscarinic M2 Receptor Human genes 0.000 description 1
108010008407 Muscarinic M2 Receptor Proteins 0.000 description 1
NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
PIJVFDBKTWXHHD-UHFFFAOYSA-N Physostigmine Natural products C12=CC(OC(=O)NC)=CC=C2N(C)C2C1(C)CCN2C PIJVFDBKTWXHHD-UHFFFAOYSA-N 0.000 description 1
241000978776 Senegalia senegal Species 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
150000004703 alkoxides Chemical class 0.000 description 1
150000001412 amines Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 1
239000011609 ammonium molybdate Substances 0.000 description 1
APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
235000018660 ammonium molybdate Nutrition 0.000 description 1
229940010552 ammonium molybdate Drugs 0.000 description 1
230000037005 anaesthesia Effects 0.000 description 1
201000007201 aphasia Diseases 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
229960000396 atropine Drugs 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
238000010876 biochemical test Methods 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
239000012267 brine Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
239000003874 central nervous system depressant Substances 0.000 description 1
210000001638 cerebellum Anatomy 0.000 description 1
210000004289 cerebral ventricle Anatomy 0.000 description 1
FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
229960001231 choline Drugs 0.000 description 1
239000000544 cholinesterase inhibitor Substances 0.000 description 1
208000004209 confusion Diseases 0.000 description 1
238000010511 deprotection reaction Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
206010013395 disorientation Diseases 0.000 description 1
230000000857 drug effect Effects 0.000 description 1
230000000350 effect on amnesia Effects 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
XIWBSOUNZWSFKU-SSDOTTSWSA-N ethyl (3r)-piperidine-3-carboxylate Chemical compound CCOC(=O)[C@@H]1CCCNC1 XIWBSOUNZWSFKU-SSDOTTSWSA-N 0.000 description 1
XIWBSOUNZWSFKU-ZETCQYMHSA-N ethyl (3s)-piperidine-3-carboxylate Chemical compound CCOC(=O)[C@H]1CCCNC1 XIWBSOUNZWSFKU-ZETCQYMHSA-N 0.000 description 1
OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000003916 ethylene diamine group Chemical group 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
230000005714 functional activity Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
QKGYJVXSKCDGOK-UHFFFAOYSA-N hexane;propan-2-ol Chemical compound CC(C)O.CCCCCC QKGYJVXSKCDGOK-UHFFFAOYSA-N 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
230000006698 induction Effects 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
201000003723 learning disability Diseases 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
239000003446 ligand Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000005948 methanesulfonyloxy group Chemical group 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000003158 myorelaxant agent Substances 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
208000015122 neurodegenerative disease Diseases 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000009871 nonspecific binding Effects 0.000 description 1
231100000956 nontoxicity Toxicity 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
238000005192 partition Methods 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
PIJVFDBKTWXHHD-HIFRSBDPSA-N physostigmine Chemical compound C12=CC(OC(=O)NC)=CC=C2N(C)[C@@H]2[C@@]1(C)CCN2C PIJVFDBKTWXHHD-HIFRSBDPSA-N 0.000 description 1
229960001697 physostigmine Drugs 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
230000002285 radioactive effect Effects 0.000 description 1
238000006462 rearrangement reaction Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
230000035939 shock Effects 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
230000009870 specific binding Effects 0.000 description 1
238000000967 suction filtration Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000820 toxicity test Toxicity 0.000 description 1
230000007704 transition Effects 0.000 description 1
OWNZHTHZRZVKSQ-UHFFFAOYSA-N tribromo(sulfanylidene)-$l^{5}-phosphane Chemical compound BrP(Br)(Br)=S OWNZHTHZRZVKSQ-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
230000001755 vocal effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Psychiatry (AREA)
Hospice & Palliative Care (AREA)
Pharmacology & Pharmacy (AREA)
Chemical Kinetics & Catalysis (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Hydrogenated Pyridines (AREA)

PT94926387T 1993-09-17 1994-09-12 Derivado de imidazolidinona opticamente activo e processo. PT719772E (pt)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP25498393		1993-09-17
JP24226494A JP3916093B2 (ja)	1993-09-17	1994-09-09	光学活性イミダゾリジノン誘導体とその製造方法

Publications (1)

Publication Number	Publication Date
PT719772E true PT719772E (pt)	2000-11-30

Family

ID=26535688

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PT94926387T PT719772E (pt)	1993-09-17	1994-09-12	Derivado de imidazolidinona opticamente activo e processo.

Country Status (15)

Country	Link
US (1)	US5726188A (da)
EP (1)	EP0719772B1 (da)
JP (1)	JP3916093B2 (da)
KR (1)	KR100323930B1 (da)
CN (1)	CN1041088C (da)
AT (1)	ATE194611T1 (da)
AU (1)	AU679259B2 (da)
CA (1)	CA2172162C (da)
DE (1)	DE69425266T2 (da)
DK (1)	DK0719772T3 (da)
ES (1)	ES2149281T3 (da)
GR (1)	GR3034499T3 (da)
HU (1)	HU217668B (da)
PT (1)	PT719772E (da)
WO (1)	WO1995007905A1 (da)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2111326T3 (es) *	1993-09-15	1998-03-01	Merck Sharp & Dohme	Derivados de imidazolona y oxazolona como antagonistas de dopamina.
US6159990A (en) *	1997-06-18	2000-12-12	Synaptic Pharmaceutical Corporation	Oxazolidinones as α1A receptor antagonists
US6316623B1 (en) *	1998-08-21	2001-11-13	Isis Pharmaceuticals, Inc.	Ethylenediamine compound libraries
US6951849B2 (en) *	2001-10-02	2005-10-04	Acadia Pharmaceuticals Inc.	Benzimidazolidinone derivatives as muscarinic agents
RU2288919C2 (ru) *	2001-10-02	2006-12-10	Акадиа Фармасьютикалз, Инк.	Производные бензимидазолидинона в качестве агентов мускариновых рецепторов
EP1960389B1 (en) *	2005-09-30	2012-08-15	Glaxo Group Limited	Compounds which have activity at m1 receptor and their uses in medicine
WO2007036711A1 (en) *	2005-09-30	2007-04-05	Glaxo Group Limited	BENZIMIDAZOLONES WHICH HAVE ACTIVITY AT Ml RECEPTOR
EA016286B1 (ru) *	2005-09-30	2012-03-30	Глэксо Груп Лимитед	Соединения, которые обладают активностью по отношению к рецепторам м, и их применения в медицине
US8338142B2 (en)	2007-02-19	2012-12-25	Kaneka Corporation	Method for producing optically active 3-aminopiperidine or salt thereof
CN102471267A (zh) *	2009-07-21	2012-05-23	住友化学株式会社	光学活性3-哌啶甲酰胺的制造方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3196152A (en) *		1965-07-20		Phenyl and alkyleneamino substituted imidazolidinones and salts thereof
US459757A (en) *		1891-09-22		Electric-arc lamp
US3355457A (en) *	1965-05-21	1967-11-28	American Cyanamid Co	Substituted 2-imidazolinones
US3459757A (en) *	1965-10-22	1969-08-05	American Cyanamid Co	Imidazolidines
US4011238A (en) *	1972-07-26	1977-03-08	Gruppo Lepetit S.P.A.	2-imidazolidione derivatives
GB9106571D0 (en) *	1991-03-27	1991-05-15	Erba Carlo Spa	Derivatives of substituted imidazol-2-one and process for their preparation
US5300515A (en) *	1991-01-31	1994-04-05	Kyorin Pharmaceutical Co., Ltd.	Carbamic acid derivatives and method for preparing the same
ES2111326T3 (es) *	1993-09-15	1998-03-01	Merck Sharp & Dohme	Derivados de imidazolona y oxazolona como antagonistas de dopamina.

1994
- 1994-09-09 JP JP24226494A patent/JP3916093B2/ja not_active Expired - Fee Related
- 1994-09-12 WO PCT/JP1994/001505 patent/WO1995007905A1/ja not_active Ceased
- 1994-09-12 EP EP94926387A patent/EP0719772B1/en not_active Expired - Lifetime
- 1994-09-12 KR KR1019960701412A patent/KR100323930B1/ko not_active Expired - Fee Related
- 1994-09-12 HU HU9600622A patent/HU217668B/hu not_active IP Right Cessation
- 1994-09-12 CN CN94194134A patent/CN1041088C/zh not_active Expired - Fee Related
- 1994-09-12 US US08/612,827 patent/US5726188A/en not_active Expired - Fee Related
- 1994-09-12 AU AU76243/94A patent/AU679259B2/en not_active Ceased
- 1994-09-12 ES ES94926387T patent/ES2149281T3/es not_active Expired - Lifetime
- 1994-09-12 DE DE69425266T patent/DE69425266T2/de not_active Expired - Fee Related
- 1994-09-12 AT AT94926387T patent/ATE194611T1/de not_active IP Right Cessation
- 1994-09-12 CA CA002172162A patent/CA2172162C/en not_active Expired - Fee Related
- 1994-09-12 DK DK94926387T patent/DK0719772T3/da active
- 1994-09-12 PT PT94926387T patent/PT719772E/pt unknown
2000
- 2000-09-28 GR GR20000402189T patent/GR3034499T3/el not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPH07133273A (ja)	1995-05-23
ES2149281T3 (es)	2000-11-01
EP0719772A1 (en)	1996-07-03
HU217668B (hu)	2000-03-28
CA2172162A1 (en)	1995-03-23
DK0719772T3 (da)	2000-11-06
EP0719772B1 (en)	2000-07-12
AU7624394A (en)	1995-04-03
WO1995007905A1 (en)	1995-03-23
CA2172162C (en)	2005-04-19
ATE194611T1 (de)	2000-07-15
AU679259B2 (en)	1997-06-26
GR3034499T3 (en)	2000-12-29
HU9600622D0 (en)	1996-05-28
CN1041088C (zh)	1998-12-09
JP3916093B2 (ja)	2007-05-16
US5726188A (en)	1998-03-10
HUT75649A (en)	1997-05-28
CN1135216A (zh)	1996-11-06
KR960704878A (ko)	1996-10-09
DE69425266D1 (de)	2000-08-17
KR100323930B1 (ko)	2004-05-06
DE69425266T2 (de)	2001-02-22
EP0719772A4 (en)	1996-09-04

Publication	Publication Date	Title
EP0468187B1 (en)	1998-03-18	Cyclic amide derivatives
JPH11501640A (ja)	1999-02-09	５−ｈｔ▲下４▼拮抗作用を有するジ−置換１，４−ピペリジンエステル類及びアミド類
EP1527048A2 (fr)	2005-05-04	Derives de n- phenyl(piperidin-2-yl)methyl benzamide, leur preparation et leur application en therapeutique
SK96194A3 (en)	1995-04-12	Bicyclic nitrogen containing compounds and pharmaceutical agents on their basis
PT91287B (pt)	1995-03-01	Processo de preparacao de derivados do acido indazol-3-carboxilico e de composicoes farmaceuticas que os contem
EP0144729B1 (en)	1989-11-08	11-Substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines, a process for their preparation and their use in medicaments
BR112013021496A2 (pt)	2019-08-06	composto, composição farmacêutica, processo para a preparação de um composto, método para o tratamento de uma desordem do sistema nervoso central
SK147897A3 (en)	1998-05-06	Azacycloalcane derivatives, preparation thereof and their applications in therapy
TWI421079B (zh)	2014-01-01	二苯并〔ｂ，ｆ〕〔１，４〕氧氮呯化合物
US5726188A (en)	1998-03-10	Optically active imidazolidinone derivatives and processes for preparing them
AU2005250197B2 (en)	2010-09-23	Tetrahydroisoquinoline sulfonamide derivatives, the preparation thereof, and the use of the same in therapeutics
JP2699511B2 (ja)	1998-01-19	置換アミン類
NO315852B1 (no)	2003-11-03	Piperazinoderivater som neurokininantagonister, farmasöytiske preparater som omfatter slike forbindelser, og anvendelse av forbindelsene tilfremstilling av medikamenter
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